The Silent Killers

Chapter 5: The Immunization Fraud, Part 1

If infection occurred every time you encountered bacteria and viruses, you would be constantly ill. Your body has built in defense mechanisms to fight off the “disease causing” germs that you come in contact with constantly, keeping you from becoming infected.

For example, all the openings into your body (nose, mouth, ears, etc.) are protected by secretions that wash away bacteria and foreign materials. Certain body fluids such as saliva and other digestive juices destroy bacteria and viruses. The hairs in your nose help to filter bacteria from the air. The tubes in your lungs are lined with little hairs that sweep bacteria and viruses from deep inside your chest up into your throat so you can cough them out. As you can see, it is not an easy task for “disease causing” microbes to get into your body.

If germs DO enter body tissues, you have even more defenses that can destroy the bacteria or viruses. Use of these defenses will render your body resistant to some infections and IMMUNE to others. Let’s take a closer look at how immunity occurs.

The protein parts of any foreign substance, such as a virus, that enter the body are called ANTIGENS. It’s important to know that the virus is never the antigen, the protein parts of it are. When this occurs, the body produces substances called ANTIBODIES. Antibodies, for the most part, are the “good guys”, antigens are the “bad guys”. The antibodies attach themselves to the invader that has the antigens on it to render them inactive. This is a very specific thing that happens. Just any antibody will not inactivate just any antigen. They fit together like lock and key. In other words, you body must manufacture specific antibodies for specific antigens, and this takes a while.

It takes a while because there must be agreement between the T-cells that recognize antigens and B-cells that make the antibodies to make absolutely sure that the antibodies will not affect proteins that are normally in the body. Unfortunately, some shots called vaccines are so potent that the numbers of antigens in them (or created by them with mRNA) can immediately cause B-cells to start making suboptimal antibodies that will affect normal body proteins. This is called autoimmune disease. The mRNA covid shots are particularly vulnerable to this because some people will use the mRNA (the message to make a protein) to make many times more protein antigens than other people will make. This variability in protein production is another reason why some people will get adverse reactions to the shot and others do not.

While your body is manufacturing antibodies, symptoms will appear IF the antigens are numerous enough and IF your body’s resistance is low enough. After the antibodies have been manufactured once, the body remembers how it manufactured those specific antibodies, and some of them are even stored for future use. Therefore, if the same antigens enter the body a second time, the body can react and destroy them more quickly, hopefully without symptoms appearing. For example, if you had measles, mumps, or chickenpox, naturally you do not expect to get them again. You will and do encounter the viruses associated with those diseases, however you do not manifest the symptoms because you now have long lasting natural immunity. This natural immunity is far superior to anything a shot called a vaccine can provide. You will get secretory IgA protection of infection as well as cross reactive T-cell protection of infection that shots cannot provide. If you do get infected you will have some stored adaptive immune system antibodies and the B-cell memory to quickly make these high quality antibodies again. This naturally induced adaptive immunity will suppress symptoms.

Now let’s think logically for a moment. If we took some viruses and made them powerful enough to cause antibodies to be formed, yet not powerful enough to produce symptoms – and injected them directly into the body; would this result in immunity? If high quality antibodies are produced, it will result in immunity called ADAPTIVE immunity because it can only adapt or react to an infection, never prevent it. Theoretically, if the correct antibodies are produced, the symptoms of the infection will be of shorter duration and less severe. This is the idea upon which the entire vaccine industry is based. But before we continue polluting the bloodstreams of America, we had better answer a couple of questions: Are vaccines safe, and do they really work?

ARE VACCINES SAFE?

There is an incredible amount of data available on the adverse effects of vaccines. The trouble is, most all the information is in medical journals instead of where it should be – before the public. When you see the commercials on television or hear doctors and nurses talk, they evade the issue. You can not believe there is another side to the story. Those who promote vaccination would have you believe that there is no controversy; and that everyone is convinced that this is the wonderful, virtuous, Christian, and heavenly way of doing it. It has become a religion where people line up in cars in church parking lots with their arms hanging out the windows waiting for their sacrament of vaccination.

There IS controversy. Vaccines are NOT inherently safe. Keep in mind that the information provided here is only the tip of the iceberg, and that the situation is actually far worse than can be written in one chapter, let alone in one book. Following are descriptions and examples of eight dangerous problems with vaccines.

1.      VARIATIONS IN THE STRENGTHS OF VACCINE DOSES

Vaccines contain viruses (or parts of viruses), so for a vaccine to do its job, the viruses in it must be potent enough to stimulate the formation of antibodies, yet not potent enough to produce the disease it is trying to prevent. This poses a very real problem, especially with “live” virus vaccines. (Some vaccines contain the entire virus, and these are called “live”, even though viruses are not living things. Some vaccines contain “killed” viruses, meaning the virus has been weakened or modified to the point where the cells in your body will not make more copies of the virus. This is sometimes called a replication defective virus). Determining and controlling the strength of a vaccine is a very difficult and expensive task.

Dr. J. Anthony Morris MD has a Ph.D. in microbiology and was trained at Walter Reed Hospital during and after World War II on infectious diseases and how they can be controlled. He was alive when I wrote this in 1984 but died in 2014 at the age of 95. You can read about him here: https://ahrp.org/john-anthony-morris-md/ In 1960 he went to the National Institute of Health to determine the risks and benefits of vaccine usage. He discovered very quickly that in many instances the risks of using vaccines outweighed the benefits.

When Dr. Morris informed the Vaccine Regulatory Authority of his findings, he was pressured to NOT publicize the information. Dr. Morris fought them and as a result the Vaccine Regulatory Authority was shown to be deficient and was reorganized. Vaccine regulation is now under a nebulous term used by the World Health Organization that is called the National Regulatory Authority (NRA) or National Control Authority (NCA), independent for each nation. Ours in the USA falls under the FDA and the Center for Biologics Evaluation and Research (CBER). Subsequently, the reorganized group was partially responsible for formulating the swine flu program that Dr. Morris strongly objected to. For objecting, he was fired after having worked in infectious diseases and the vaccine field for the federal government for several years.

During his vaccine research, Dr. Morris found that there was NO WAY to reliably control the potency of vaccines. No matter what the labels on the vaccine batches said, the strengths of the doses might vary. This is still a problem today. The active particles in the Covid-19 shot can vary ten-fold from syringe to syringe dependent upon how it was stored and mixed.

Let’s look at how this problem of potency variation affected the polio vaccine. There was an incident in the mid 1950’s in which polio virus vaccines made by Cutter in California, resulted in polio developing in children. It all started when the National Foundation for Infantile Paralysis made a series of requests to the American public to create a program to control polio in this country. The March of Dimes was formed, and literally millions of dollars were contributed each year to the national foundation in an attempt to develop a polio virus vaccine.

Indeed, Dr. Jonas Salk was successful in developing such a vaccine. So, the National Institute of Health (NIH) went to congress and asked for millions of dollars to fund a vaccination program, and congress appropriated that money by which the goal could be accomplished.

AFTER the program was well underway, a scientist at the NIH learned that some of the lots of polio virus released to the public caused paralysis in monkeys. Note: Animal testing should always be done in vaccine trials. With the polio shot it was done too late, with the Covid-19 shot, animal trials were completely skipped. In other words, the viruses in the vaccine had not lost their ability to produce polio. These facts were made known to the NIH administrators. They completely ignored the information and the person who discovered this problem was told to NOT make it public. Subsequently, some of those lots went into children, they developed polio, and the program had to come to a halt.

You may be wondering why the program was not halted when the monkeys became paralyzed at the onset. It was not done for a purely political reason. The NIH administrators gave the official word to congress that the vaccine was “safe, effective, and would do away with polio in this country.” After making that great promise, it was very difficult politically for the administrators of NIH to go back to congress and say, “Oops, we made a mistake; we have a problem this vaccine that should be corrected, and we would like to hold up for six months or so until the situation is clarified”. That was not done, and as a result several cases of polio in children occurred. Unfortunately, Cutter Laboratories had to apologize for the mistake and look like the villain, when actually the disaster resulted from screw-ups in governmental direction and supervision. Are you paying attention, Fauci?

Here is another illustration of how the problem of potency variation can affect vaccines. Picture what a child with the measles looks like. Following is an example of what the little card says, the one they give you at the public health clinics if you take your child in for an MMR shot: “The shot your child just received will provide protection from seven day measles, three day measles and mumps. After today’s vaccination you might notice that there might be a mild fever from the rubella portion of the shot. Approximately seven to ten days after the vaccination your child may have a day or two of fever from the measles portions of the shot. Some children may run a fever as high as 102 degrees. Liquid baby aspirin may be given according to the directions for your child’s age. If the fever continues or gets higher than 102, you should contact the clinic or your family doctor. During this time, your child might show a slight rash; a few spots usually on the chest. This should not be bothersome and requires no treatment.”

Now, you tell me what the symptoms of measles are. This is abnormal infectivity. The vaccine is so potent that it allows the disease symptoms to manifest that it is supposed to prevent.

Here we are in 2022 and potency variation is still a problem, now with the covid shot. Billions of vials were mixed and shipped all over the world. After delivery there are very strict rules for time and temperature of storage. Then some of the doses must be mixed and diluted a very precise way prior to injection. As mentioned already, the potency can vary by tenfold. This is only one of many reasons why some people get adverse reactions to the shot and others do not. It’s a crapshoot. How lucky do you feel?